Canonical Allele Identifier: CA1118879474
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1813380827

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527712_125527713insA , CM000670.2:g.125527712_125527713insA GRCh38
NC_000008.10:g.126539954_126539955insA , CM000670.1:g.126539954_126539955insA GRCh37
NC_000008.9:g.126609136_126609137insA NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54398_256+54399insA
XR_001746072.1:n.583+4699_583+4700insA
XR_001746073.1:n.583+4699_583+4700insA